| Literature DB >> 11398894 |
J Volk1, F Reinke, A B van Kuilenburg, A H van Gennip, C Schlichting, A Ganser, P Schöffski.
Abstract
Dihydropyrimidine dehydrogenase deficiency is diagnosed more frequently and is now generally accepted as a potentially life-threatening condition. It predisposes patients receiving treatment with fluoropyrimidines such as 5-fluorouracil (5-FU) to severe and, in case of complete dihydropyrimidine dehydrogenase deficiency, often fatal toxicity. A patient who had severe side effects following standard dose adjuvant 5-FU exposure was diagnosed of having hereditary partial dihydropyrimidine dehydrogenase deficiency. When the patient relapsed with liver metastases, we treated him with the non-fluoropyrimidine cytotoxic agents irinotecan, oxaliplatin and raltitrexed in sequential manner, and were able to show that these drugs can be safely applied in patients with this metabolic defect.Entities:
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Year: 2001 PMID: 11398894 DOI: 10.1023/a:1011178111295
Source DB: PubMed Journal: Ann Oncol ISSN: 0923-7534 Impact factor: 32.976